
Euroimmun Us, Inc.
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EUROIMMUN IFA: Crithidia luciliae (anti-dsDNA) EUROPattern is an FDA 510(k)-cleared medical device (K172244) manufactured by Euroimmun Us, Inc.. This device is classified under the Immunology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 19, 2018. Regulation: 8.